Water Attachment onto Size-Selected Cationic Hydroxy–Pyrene Clusters

Abstract We study the attachment of a single water molecule colliding with cationic clusters of hydroxypyrene (PyOH)─a medium-sized hydroxylated polycyclic aromatic hydrocarbon (OH-PAH). The (PyOH)n+ clusters (n = 2–6) were generated using a cryogenic molecular cluster source. The attachment rates are measured as a function of collision energy and initial cluster temperature. To rationalize the experimental results, we use a model that accounts for the dissociation rates of the water molecule in [(PyOH)nH2O]+ complexes to estimate the survival probability of these species. The derived binding energies range from ∼0.5 to 0.4 eV, decreasing with cluster size. By comparing our results with a previous study on pyrene clusters, we highlight the key role of charge combined with the hydroxyl function in enhancing the stability of [(PyOH)nH2O]+ complexes at higher temperatures. These findings add a new piece to the chemical network driving the physico-chemical evolution of PAHs and their role in planet-forming regions and exoplanetary atmospheres.

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Journal
The Journal of Physical Chemistry A
Published
2026-09-21
DOI
https://doi.org/10.1021/acs.jpca.6c05183
Primary Topic
Astrophysics and Star Formation Studies
Type
article
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article

Water Attachment onto Size-Selected Cationic Hydroxy–Pyrene Clusters

Aude Simon, Sébastien Zamith, A. Marciniak, C. Joblin et al.
The Journal of Physical Chemistry A
Astrophysics and Star Formation Studies
article

Water Attachment onto Size-Selected Cationic Hydroxy–Pyrene Clusters

Aude Simon, Sébastien Zamith, A. Marciniak, C. Joblin, Fatima Baterdouk
article en

Abstract

Abstract We study the attachment of a single water molecule colliding with cationic clusters of hydroxypyrene (PyOH)─a medium-sized hydroxylated polycyclic aromatic hydrocarbon (OH-PAH). The (PyOH)n+ clusters (n = 2–6) were generated using a cryogenic molecular cluster source. The attachment rates are measured as a function of collision energy and initial cluster temperature. To rationalize the experimental results, we use a model that accounts for the dissociation rates of the water molecule in [(PyOH)nH2O]+ complexes to estimate the survival probability of these species. The derived binding energies range from ∼0.5 to 0.4 eV, decreasing with cluster size. By comparing our results with a previous study on pyrene clusters, we highlight the key role of charge combined with the hydroxyl function in enhancing the stability of [(PyOH)nH2O]+ complexes at higher temperatures. These findings add a new piece to the chemical network driving the physico-chemical evolution of PAHs and their role in planet-forming regions and exoplanetary atmospheres.

The Journal of Physical Chemistry A
Centre National de la Recherche Scientifique (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR)
Openalex Percentile: Top 10%
Astrophysics and Star Formation Studies
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